Targeted Therapy

EMA Backs Targeted Akeega Therapy for BRCA-Mutated Prostate Cancer

European regulators have given a positive recommendation to expand the use of Akeega, a combination of niraparib and abiraterone, for patients with metastatic hormone-sensitive prostate cancer who carry BRCA1 or BRCA2 mutations. If approved, this pill—taken with prednisone and standard hormone therapy—would offer a targeted treatment option earlier in the disease, based on a patient’s […]

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New Drug Exploits Hidden Weakness in Pancreatic Cancer Cells, Showing Early Promise

Researchers have identified a new vulnerability in pancreatic ductal adenocarcinoma, the most common and aggressive type of pancreatic cancer, by focusing on transcription–replication conflicts. In cancer cells, the machinery that reads genes and the machinery that copies DNA can collide, causing stress and DNA damage. These collisions are especially frequent in pancreatic cancer cells with

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MUC18-Targeted ADC AMT-253 Shows Strong Early Efficacy in Melanoma and Gynecologic Cancers

AMT-253, a MUC18-targeted antibody-drug conjugate, has shown encouraging results in two phase 1 melanoma studies. Among 56 evaluable melanoma patients, the overall response rate was 28.6%, with 15 confirmed partial responses, and the disease control rate reached 73.2%. Responses varied by melanoma subtype, with acral and unknown primary melanoma showing particularly strong disease control. Patients

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Astatine-211 Production for Next-Generation Targeted Cancer Therapy

Scientists have developed a new way to produce, isolate, and ship astatine-211 (At-211), a rare and unstable radioactive isotope with strong potential for targeted cancer therapy. Known as a “Goldilocks isotope,” At-211 is considered ideal for cancer treatment because it delivers powerful, localized bursts of energy that can kill cancer cells without harming nearby healthy

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FDA Approves First Targeted Therapy for IDH-Mutant Low-Grade Glioma

The FDA has approved vorasidenib, the first targeted drug for people with Grade 2 diffuse glioma that carries an IDH1 or IDH2 mutation. This marks an important advance for a slow-growing but incurable brain cancer. About 3,500 Americans are diagnosed with this type of tumor each year. Most cases (70–80%) have an IDH1 mutation. Patients

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New Protein Target May Stop Early Drug Resistance in EGFR-Mutant Lung Cancer

A Researchers have uncovered how lung cancer rapidly develops resistance to osimertinib, a key drug for EGFR-mutant tumors. Resistance can emerge within six to eight weeks of starting treatment, earlier than previously thought. The study identified a protein, METTL7A, as a critical driver of this process. METTL7A remodels chromatin, making it easier for cancer cells

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New Research Highlights Nuclear Receptors as Promising Targets in Brain Cancer Treatment

Brain cancer continues to be a major global health burden. Patients often experience persistent headaches, seizures, memory loss, and difficulty thinking, which significantly affect quality of life. Glioblastoma (GBM) is the most common and deadliest type of brain tumor. It grows rapidly, infiltrates normal brain tissue, and is very difficult to treat. Standard care includes surgery

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Major Advances in Targeted Therapies Transform Treatment for Blood Cancers

There have been major advances in targeted therapies for blood cancers, especially chronic lymphocytic leukemia (CLL), large B-cell lymphoma (LBCL), and myelofibrosis (MF). In CLL, treatment has largely shifted from chemotherapy to BTK inhibitors. Newer drugs like acalabrutinib (Calquence) and zanubrutinib (Brukinsa) provide strong, lasting responses with fewer side effects than older drugs such as

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Targeting Lactylation Offers New Hope for Treatment-Resistant Cancers

Cancer cells often rely on an inefficient energy process known as the Warburg effect, where glucose is converted to lactate even in the presence of oxygen. This excess lactate is not merely waste—it fuels an epigenetic process called lactylation. In lactylation, lactate is transformed into lactyl-CoA and attached to lysine residues on histone and non-histone

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Stopping the Spread: EZH2 Inhibitors Thwart Aggressive Breast Cancer Metastasis

A new study from Weill Cornell Medicine reveals that the enzyme EZH2 drives chromosomal instability in triple-negative breast cancer (TNBC), promoting metastasis. Researchers found that overproduction of EZH2 silences the gene tankyrase 1, causing accumulation of CPAP and abnormal chromosome segregation during cell division. This faulty process enables cancer cells to spread aggressively to distant organs.

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